Literature DB >> 16100619

Dinitroso and polynitroso compounds.

Brian G Gowenlock1, George B Richter-Addo.   

Abstract

The growing interest in the chemistry of C-nitroso compounds (RN=O; R = alkyl or aryl group) is due in part to the recognition of their participation in various metabolic processes of nitrogen-containing compounds. C-Nitroso compounds have a rich organic chemistry in their own right, displaying interesting intra- and intermolecular dimerization processes and addition reactions with unsaturated compounds. In addition, they have a fascinating coordination chemistry. While most of the attention has been directed towards C-nitroso compounds containing a single -NO moiety, there is an emerging area of research dealing with dinitroso and polynitroso compounds. In this critical review, we present and discuss the synthetic routes and properties of these relatively unexplored dinitroso and polynitroso compounds, and suggest areas of further development involving these compounds. (126 references.).

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Year:  2005        PMID: 16100619      PMCID: PMC1574367          DOI: 10.1039/b500855g

Source DB:  PubMed          Journal:  Chem Soc Rev        ISSN: 0306-0012            Impact factor:   54.564


  12 in total

Review 1.  Interactions of organic nitroso compounds with metals.

Authors:  Jonghyuk Lee; Li Chen; Ann H West; George B Richter-Addo
Journal:  Chem Rev       Date:  2002-04       Impact factor: 60.622

Review 2.  Nitric oxide donors: chemical activities and biological applications.

Authors:  Peng George Wang; Ming Xian; Xiaoping Tang; Xuejun Wu; Zhong Wen; Tingwei Cai; Adam J Janczuk
Journal:  Chem Rev       Date:  2002-04       Impact factor: 60.622

Review 3.  The nitroso ene reaction: a regioselective and stereoselective allylic nitrogen functionalization of mechanistic delight and synthetic potential.

Authors:  Waldemar Adam; Oliver Krebs
Journal:  Chem Rev       Date:  2003-10       Impact factor: 60.622

Review 4.  Preparations of C-nitroso compounds.

Authors:  Brian G Gowenlock; George B Richter-Addo
Journal:  Chem Rev       Date:  2004-07       Impact factor: 60.622

5.  Viriplanin A, a new anthracycline antibiotic of the nogalamycin group. I. Isolation, characterization, degradation reactions and biological properties.

Authors:  K Hütter; E Baader; K Frobel; A Zeeck; K Bauer; W Gau; J Kurz; T Schröder; C Wünsche; W Karl
Journal:  J Antibiot (Tokyo)       Date:  1986-09       Impact factor: 2.649

6.  Blue alkali dinitrosomethanides: synthesis, structure, and bonding.

Authors:  Harald Brand; Peter Mayer; Kurt Polborn; Axel Schulz; Jan J Weigand
Journal:  J Am Chem Soc       Date:  2005-02-09       Impact factor: 15.419

7.  Nitrosoalkenes: Synthesis and Properties of Nitroso Derivatives of a Vinylogous Tetrathiafulvalene.

Authors:  Yvette A. Jackson; James P. Parakka; M. V. Lakshmikantham; Michael P. Cava
Journal:  J Org Chem       Date:  1997-04-18       Impact factor: 4.354

8.  Dimerizations of nitrile oxides to furoxans are stepwise via dinitrosoalkene diradicals: a density functional theory study.

Authors:  Zhi-Xiang Yu; Pierluigi Caramella; K N Houk
Journal:  J Am Chem Soc       Date:  2003-12-17       Impact factor: 15.419

9.  Protorubradirin, an antibiotic containing a C-nitroso-sugar fragment, is the true secondary metabolite produced by Streptomyces achromogenes var. rubradiris. Rubradirin, described earlier, is its photo-oxidation product.

Authors:  B Bannister; B A Zapotocky
Journal:  J Antibiot (Tokyo)       Date:  1992-08       Impact factor: 2.649

10.  Viriplanin A, a new anthracycline antibiotic of the nogalamycin group. II. The structure of a novel hydroxyamino sugar from reduced viriplanin A.

Authors:  R Kind; K Hütter; A Zeeck; K Schmidt-Bäse; E Egert
Journal:  J Antibiot (Tokyo)       Date:  1989-01       Impact factor: 2.649

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  2 in total

1.  Constructing monocrystalline covalent organic networks by polymerization.

Authors:  Daniel Beaudoin; Thierry Maris; James D Wuest
Journal:  Nat Chem       Date:  2013-08-25       Impact factor: 24.427

2.  Crystal engineering: Covalent crystal growth.

Authors:  Michael Mastalerz
Journal:  Nat Chem       Date:  2013-10       Impact factor: 24.427

  2 in total

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